Luan Xinhong, Liu Dawei, Cao Zhongzan, Luo Lina, Liu Mei, Gao Ming, Zhang Xiaoying
College of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang, 110866, China.
Liaoning Province Livestock and Poultry Genetic Resources Conservation and Utilization Center, Liaoyang, 111000, China.
PLoS One. 2014 Nov 24;9(11):e113211. doi: 10.1371/journal.pone.0113211. eCollection 2014.
The Huoyan goose is famous for its high egg-laying performance and is listed as a nationally protected domestic animal by the Chinese government. To elucidate the key regulatory genes involved in Huoyan goose egg laying, RNA from ovarian tissue during the ceased and laying periods was sequenced using the Illumina HiSeq 2000 sequencing platform. More than 12 million reads were produced in ceased and laying libraries that included 11,896,423 and 12,534,799 clean reads, respectively. More than 20% of the reads were matched to the reference genome, and 23% of the reads were matched to reference genes. Genes with a false discovery rate (FDR) ≤0.001 and log2ratio ≧1 or ≤-1 were characterized as differentially expressed, and 344 up-regulated and 344 down-regulated genes were classified into functional categories. Twelve genes that are mainly involved in pathways for reproduction regulation, such as steroid hormone biosynthesis, GnRH signaling pathways, oocyte meiosis, progesterone-mediated oocyte maturation, steroid biosynthesis, calcium signaling pathways, and G-protein coupled receptor signaling pathway were selected for validation by a quantitative real-time polymerase chain reaction (qRT-PCR) analysis, the qRT-PCR results are consistent with the general expression patterns of those genes from the Illumina sequencing. These data provide comprehensive gene expression information at the transcriptional level that might increase our understanding of the Huoyan goose's reproductive biology.
豁眼鹅以其高产蛋性能而闻名,被中国政府列为国家保护家禽。为了阐明参与豁眼鹅产蛋的关键调控基因,利用Illumina HiSeq 2000测序平台对停产期和产蛋期卵巢组织的RNA进行了测序。停产期文库和产蛋期文库分别产生了超过1200万条读数,其中包括11896423条和12534799条clean reads。超过20%的读数与参考基因组匹配,23%的读数与参考基因匹配。错误发现率(FDR)≤0.001且log2ratio≧1或≤-1的基因被鉴定为差异表达基因,344个上调基因和344个下调基因被分类到功能类别中。选择了12个主要参与生殖调控途径的基因,如类固醇激素生物合成、GnRH信号通路、卵母细胞减数分裂、孕酮介导的卵母细胞成熟、类固醇生物合成、钙信号通路和G蛋白偶联受体信号通路,通过定量实时聚合酶链反应(qRT-PCR)分析进行验证,qRT-PCR结果与Illumina测序中这些基因的总体表达模式一致。这些数据提供了转录水平上全面的基因表达信息,可能会增加我们对豁眼鹅生殖生物学的理解。